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1-benzyl-4-(2-methoxymethoxy-phenyl)-piperidine-4-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73406-58-3

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73406-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73406-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,0 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73406-58:
(7*7)+(6*3)+(5*4)+(4*0)+(3*6)+(2*5)+(1*8)=123
123 % 10 = 3
So 73406-58-3 is a valid CAS Registry Number.

73406-58-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-4-(2-methoxymethoxy-phenyl)-piperidine-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 1-Benzyl-4-cyano-4-(2-methoxymethoxyphenyl)-piperidin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:73406-58-3 SDS

73406-58-3Upstream product

73406-58-3Relevant academic research and scientific papers

Synthesis and hydrolysis kinetics of 4-cyano-4-phenylpiperidine derivatives: A route to morphine analogs

Gervais,Anker,Chareire,Pacheco

, p. 241 - 248 (2007/10/05)

A description is given of a high-yield synthesis leading to various hydroxy-2 phenylacetonitriles and to various benzodihydro-2,3 furannones-2. The intermediary 12 benzylic mesylates give quantitatively the corresponding 11 chlorides by the action of hydrochlorate of triethylamine; this procedure constitutes a very rewarding and easy method for chlorinating the benzylic alcohols in two stages without isolating the intermediary. A proximate effect has been shown which makes possible the hydrolysis of certain phenylacetonitriles by dilute acetic acid. This hydrolysis becomes very rapid when these nitriles are distributed; the increase of the speed of the hydrolysis illustrates the gem dialkyle effect.

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